PIK3CA assay guides treatment of progressing breast cancer
Answers from the Lab
Katherine Geiersbach, M.D., explains how Mayo Clinic Laboratories' PIK3CA assay informs treatment for recurrent or progressing breast cancer. The assay identifies patients eligible for a certain second-line therapy when initial hormonal treatment has failed.
PIK3CA is a mutation present in 40% of breast cancers. In this test specific episode of the "Answers From the Lab" podcast, Katherine Geiersbach, M.D., explains how Mayo Clinic Laboratories' PIK3CA assay guides treatment decisions for certain types of breast cancer.
"The PIK3CA mutation test is used to determine eligibility for a kinase inhibitor treatment in a subset of patients with breast cancer," Dr. Geiersbach says. That subset is postmenopausal women or men who have hormone receptor-positive breast cancer that has progressed despite endocrine-based therapy. The kinase inhibitor, known as alpelisid, targets the PIK3CA mutation.
Mayo Clinic Laboratories offers PIK3CA testing using both breast tumor tissue and plasma. Dr. Geiersbach notes that most oncologists prefer tissue testing because the fraction of circulating tumor DNA in plasma may be low.
"It's important to have accurate and sensitive PIK3CA testing to select patients who would benefit from therapy and also to accurately detect the PIK3CA-negative patients who wouldn't benefit and might have toxicity from the therapy," Dr. Geiersbach says.
Listen to learn more about Mayo Clinic Laboratories' PIK3CA testing.
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PIK3B | Cell-Free DNA PIK3CA Test, Blood
PIK3T | PIK3CA Mutation Analysis, Tumor
PIK3B | Cell-Free DNA PIK3CA Test, Blood
Identification of hormone receptor positive and human epidermal growth factor receptor 2 negative (HR+/HER2-) advanced breast cancer tumors that may be eligible for treatment with targeted kinase inhibitor therapy (eg, alpelisib).
PIK3T | PIK3CA Mutation Analysis, Tumor
Identification of hormone receptor positive and human epidermal growth factor receptor 2 negative (HR+/HER2-) advanced breast cancer tumors that may be eligible for treatment with targeted kinase inhibitor therapy (eg, alpelisib).
PIK3B | Cell-Free DNA PIK3CA Test, Blood
Additional Information:
PIK3T | PIK3CA Mutation Analysis, Tumor
NECESSARY INFORMATION:
A pathology report (final or preliminary), at minimum containing the following information, must accompany specimen for testing to be performed:
SPECIMEN REQUIRED
This assay requires at least 20% tumor nuclei.
The amount of tissue needed is dependent on a variety of preanalytical factors (eg, cellularity, ischemic time, fixation). The FFPE input required is equivalent to a 4 to 5 micron slide thickness with a total tumor surface area of 100 mm(2). This can be created by combining material from multiple slides from one tissue block.
Preferred:
Acceptable:
PIK3B | Cell-Free DNA PIK3CA Test, Blood
Analytic time: 5 to 10 days
Days performed: Monday through Friday
PIK3T | PIK3CA Mutation Analysis, Tumor
Analytic time: 8 to 12 days
Days performed: Monday through Friday